NP-MRD: Showing NP-Card for (-)-Leucasdin A (NP0071432)

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Record Information

Version

2.0

Created at

2022-04-28 16:48:56 UTC

Updated at

2022-04-28 16:48:56 UTC

NP-MRD ID

NP0071432

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Leucasdin A

Description

Leucasdin A belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (-)-Leucasdin A is found in Leucas cephalotes and Leucas cephalotes SPRENG. . Based on a literature review very few articles have been published on Leucasdin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282218482D          

 33 36  0  0  1  0            999 V2000
    2.4565    1.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1628    3.2700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.7567    3.0156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652304282218482D          

 33 36  0  0  1  0            999 V2000
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M  END
> <DATABASE_ID>
NP0071432

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H](OC=O)[C@H]2C(C)(C)[C@H](CC[C@]2(C)[C@@]11CC[C@@]2(CCO[C@H]2OC(C)=O)O1)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O8/c1-15-13-18(30-14-26)20-22(4,5)19(31-16(2)27)7-8-23(20,6)25(15)10-9-24(33-25)11-12-29-21(24)32-17(3)28/h14-15,18-21H,7-13H2,1-6H3/t15-,18-,19+,20+,21+,23+,24+,25-/m1/s1

> <INCHI_KEY>
WZISBLRBOQCBRZ-ZFGSYAMDSA-N

> <FORMULA>
C25H38O8

> <MOLECULAR_WEIGHT>
466.571

> <EXACT_MASS>
466.256668184

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
49.59167563655737

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,2''S,4R,4aS,5'S,6S,8aS)-2''-(acetyloxy)-4-(formyloxy)-2,5,5,8a-tetramethyl-octahydro-2H-dispiro[naphthalene-1,2':5',3''-bis(oxolane)]-6-yl acetate

> <ALOGPS_LOGP>
3.07

> <JCHEM_LOGP>
2.856702177999999

> <ALOGPS_LOGS>
-5.18

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.991636457028678

> <JCHEM_POLAR_SURFACE_AREA>
97.36000000000001

> <JCHEM_REFRACTIVITY>
116.37229999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.11e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,2''S,4R,4aS,5'S,6S,8aS)-2''-(acetyloxy)-4-(formyloxy)-2,5,5,8a-tetramethyl-hexahydro-2H-dispiro[naphthalene-1,2':5',3''-bis(oxolane)]-6-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       4.585   3.073   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.761   4.068   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.487   5.584   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.037   6.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.862   5.109   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.136   3.593   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.412   5.629   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.138   7.145   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.314   8.140   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.763   7.619   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.939   8.614   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.664  10.130   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.840  11.125   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.311   7.665   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.527   4.093   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.101   3.510   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.894   4.686   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.083   5.995   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.704   3.376   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.200   3.742   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.314   5.278   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.889   5.861   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.121   1.951   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.064   0.733   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.481  -0.692   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.590   0.941   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.052   3.799   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.992   5.910   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.057   7.014   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.210   3.548   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.484   2.032   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.934   1.512   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.309   1.037   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   30                                                  
CONECT    3    2    4   28   29                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   27                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   15   18                                             
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    8                                                            
CONECT   15    7   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   22                                             
CONECT   18   17    7                                                       
CONECT   19   17   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   19   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    5                                                            
CONECT   28    3                                                            
CONECT   29    3                                                            
CONECT   30    2   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₈O₈

Average Mass

466.5710 Da

Monoisotopic Mass

466.25667 Da

IUPAC Name

(1R,2R,2''S,4R,4aS,5'S,6S,8aS)-2''-(acetyloxy)-4-(formyloxy)-2,5,5,8a-tetramethyl-octahydro-2H-dispiro[naphthalene-1,2':5',3''-bis(oxolane)]-6-yl acetate

Traditional Name

(1R,2R,2''S,4R,4aS,5'S,6S,8aS)-2''-(acetyloxy)-4-(formyloxy)-2,5,5,8a-tetramethyl-hexahydro-2H-dispiro[naphthalene-1,2':5',3''-bis(oxolane)]-6-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H](OC=O)[C@H]2C(C)(C)[C@H](CC[C@]2(C)[C@@]11CC[C@@]2(CCO[C@H]2OC(C)=O)O1)OC(C)=O

InChI Identifier

InChI=1S/C25H38O8/c1-15-13-18(30-14-26)20-22(4,5)19(31-16(2)27)7-8-23(20,6)25(15)10-9-24(33-25)11-12-29-21(24)32-17(3)28/h14-15,18-21H,7-13H2,1-6H3/t15-,18-,19+,20+,21+,23+,24+,25-/m1/s1

InChI Key

WZISBLRBOQCBRZ-ZFGSYAMDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Leucas cephalotes	LOTUS Database	35616633
Leucas cephalotes SPRENG.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Grindelane diterpenoid
Tricarboxylic acid or derivatives
Tetrahydrofuran
Carboxylic acid ester
Acetal
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.07	ALOGPS
logP	2.86	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	97.36 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	116.37 m³·mol⁻¹	ChemAxon
Polarizability	49.59 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00030652

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91516665

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-Leucasdin A (NP0071432)

MOL for NP0071432 ((-)-Leucasdin A)

3D MOL for NP0071432 ((-)-Leucasdin A)

3D SDF for NP0071432 ((-)-Leucasdin A)

3D-SDF for NP0071432 ((-)-Leucasdin A)

PDB for NP0071432 ((-)-Leucasdin A)

3D PDB for NP0071432 ((-)-Leucasdin A)

SMILES for NP0071432 ((-)-Leucasdin A)

INCHI for NP0071432 ((-)-Leucasdin A)

Structure for NP0071432 ((-)-Leucasdin A)

3D Structure for NP0071432 ((-)-Leucasdin A)